EP4132894B1 - Verfahren zur herstellung eines dekorierten, mineralischen verbundkörpers, dekorierter, mineralischer verbundkörper und verwendung einer mehrschichtfolie - Google Patents

Verfahren zur herstellung eines dekorierten, mineralischen verbundkörpers, dekorierter, mineralischer verbundkörper und verwendung einer mehrschichtfolie Download PDF

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Publication number
EP4132894B1
EP4132894B1 EP21713902.1A EP21713902A EP4132894B1 EP 4132894 B1 EP4132894 B1 EP 4132894B1 EP 21713902 A EP21713902 A EP 21713902A EP 4132894 B1 EP4132894 B1 EP 4132894B1
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EP
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Prior art keywords
group
mineral
layer
polymer
decorated
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EP21713902.1A
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German (de)
English (en)
French (fr)
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EP4132894A1 (de
Inventor
Uwe Reuther
Roman LASCH
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Leonhard Kurz Stiftung and Co KG
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Leonhard Kurz Stiftung and Co KG
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    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/4505—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements characterised by the method of application
    • C04B41/4511—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements characterised by the method of application using temporarily supports, e.g. decalcomania transfers or mould surfaces
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B28—WORKING CEMENT, CLAY, OR STONE
    • B28B—SHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B19/00—Machines or methods for applying the material to surfaces to form a permanent layer thereon
    • B28B19/0015—Machines or methods for applying the material to surfaces to form a permanent layer thereon on multilayered articles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B13/00—Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material
    • B32B13/04—Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material comprising such water setting substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B13/12—Layered products comprising a a layer of water-setting substance, e.g. concrete, plaster, asbestos cement, or like builders' material comprising such water setting substance as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B44—DECORATIVE ARTS
    • B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
    • B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
    • B44C1/16—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like
    • B44C1/165—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like for decalcomanias; sheet material therefor
    • B44C1/17—Dry transfer
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B44—DECORATIVE ARTS
    • B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
    • B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
    • B44C1/16—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like
    • B44C1/165—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like for decalcomanias; sheet material therefor
    • B44C1/17—Dry transfer
    • B44C1/1708—Decalcomanias provided with a layer being specially adapted to facilitate their release from a temporary carrier
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B44—DECORATIVE ARTS
    • B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
    • B44C5/00—Processes for producing special ornamental bodies
    • B44C5/04—Ornamental plaques, e.g. decorative panels, decorative veneers
    • B44C5/0453—Ornamental plaques, e.g. decorative panels, decorative veneers produced by processes involving moulding
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/02—Granular materials, e.g. microballoons
    • C04B14/04—Silica-rich materials; Silicates
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/001—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing unburned clay
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/18—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/18—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type
    • C04B28/186—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type containing formed Ca-silicates before the final hardening step
    • C04B28/188—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type containing formed Ca-silicates before the final hardening step the Ca-silicates being present in the starting mixture
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/4578—Coating or impregnating of green ceramics or unset concrete
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
    • C04B41/48—Macromolecular compounds
    • C04B41/4857—Other macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B41/4873—Polyvinylacetals
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/52—Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/52—Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
    • C04B41/522—Multiple coatings, for one of the coatings of which at least one alternative is described
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
    • C04B41/61—Coating or impregnation
    • C04B41/62—Coating or impregnation with organic materials
    • C04B41/63—Macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
    • C04B41/61—Coating or impregnation
    • C04B41/70—Coating or impregnation for obtaining at least two superposed coatings having different compositions
    • C04B41/71—Coating or impregnation for obtaining at least two superposed coatings having different compositions at least one coating being an organic material
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2451/00—Decorative or ornamental articles
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/20—Resistance against chemical, physical or biological attack
    • C04B2111/28—Fire resistance, i.e. materials resistant to accidental fires or high temperatures
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/60—Flooring materials
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/60—Flooring materials
    • C04B2111/62—Self-levelling compositions

Definitions

  • a multi-layer film to be used according to the invention which can preferably be designed as a transfer film or laminating film, comprises a carrier layer and a transfer layer arranged on the carrier layer, which contains at least one decorative element, the transfer layer being arranged on the carrier layer, preferably detachably, when the multi-layer film is designed as a transfer film.
  • the transfer layer is preferably arranged firmly and inseparably on the carrier layer.
  • the carrier layer is preferably removed from the transfer layer, preferably completely, so that only the transfer layer is arranged on at least partial areas of the surface of the decorated object, preferably at least partially forms the surface of the decorated object.
  • the transfer layer arranged on at least partial areas of the surface of the decorated object preferably forms a, more preferably closed, coating.
  • the detachment of the carrier layer from the transfer layer preferably takes place at a layer boundary between the carrier layer and the transfer layer.
  • a detachment layer can be arranged at this layer boundary, which facilitates the detachment of the transfer layer from the carrier layer.
  • the release layer can be part of the transfer layer and/or part of the carrier film and can be arranged on the transfer layer and/or on the carrier film after detachment.
  • the multilayer film designed as a laminating film can, for example, after the multilayer film has been arranged on at least partial areas of the at least one surface of the decorated object, enable two or more objects decorated according to the invention to be connected, for example with the aid of joining by forming and/or joining under the influence of heat and /or pressure, in which case preferably two or more adjacent multilayer films can be connected, for example by welding, gluing, hot stamping, laminating or combinations thereof.
  • At least one decorative element is transferred to the object together with the transfer layer, with the at least one decorative element being arranged on at least partial areas of the surface of the decorated object after the transfer layer has been transferred and, depending on the design of the at least one decorative element, the physical properties, preferably the haptic properties and/or the optical and/or the electrical and/or the mechanical properties and/or the chemical properties of the surface of the decorated object.
  • the at least one decorative element can change the surface texture and/or color of the decorated object, for example by providing embossing and/or roughening and/or patterns and/or smoothness and/or by providing reflection-determining properties such as transparency and/or gloss and/or or matting and/or by providing a color.
  • the at least one decorative element can influence the mechanical properties of the decorated object, for example by providing surface hardness, surface elasticity and/or breaking strength of the surface.
  • the at least one decorative element can influence the capacity and/or permeability of the decorated object for water and/or water vapor, for example by providing a water- and/or water-vapour-repellent coating.
  • the at least one decorative element can be in the form of an optically active and/or optically variable substance, which is preferably present as a dye, liquid crystal material, pigment or a mixture thereof.
  • Suitable pigments are, for example, interference layer pigments, liquid crystal pigments, diffractive pigments, metallic pigments, thermochromic pigments, photochromic pigments or mixtures thereof.
  • the substance can show different or similar optical effects in different wavelength ranges, for example in the infrared range and/or in the ultraviolet range and/or in the visible range.
  • the substance can also show different or similar optical effects under different lighting and/or viewing angles or directions.
  • the decorative element preferably has at least one decorative layer.
  • the decorative element preferably has a number of decorative layers.
  • the at least one decorative layer preferably includes or consists independently of one another of at least partially arranged, preferably full-surface, protective layers, at least partially arranged barrier layers, at least partially arranged reflection layers, at least partially arranged conductive layers, at least partially arranged adhesion promoter layers, at least partially arranged adhesive layers, at least partially arranged metal layers , at least partially arranged layers with relief structures, at least partially arranged color layers, at least partially arranged interference layers or combinations thereof.
  • the at least one decorative layer can preferably be opaque and/or translucent and/or transparent at least in regions.
  • the decorative layers can each have different degrees of transparency independently of one another.
  • the at least one decorative layer from the group consisting of transparent and/or colored lacquer layers, in particular comprising one or more dyes and/or pigments, replication layers with a molded optically active surface structure, reflection layers, in particular opaque reflection layers, transparent reflection layers, metallic Reflective layers or dielectric reflective layers, optically variable layers, optically active layers, interference multilayer systems, volume hologram layers, liquid crystal layers, in particular cholesteric liquid crystal layers, electrically conductive layers, antenna layers, electrode layers, magnetic layers, magnetic storage layers, barrier layers and combinations thereof.
  • the inventors have found that by upgrading a mineral building material with at least one multilayer film to be used according to the invention, the occurrence of corrosion, for example concrete corrosion, can be prevented.
  • a chemical reaction that takes place in concrete in the presence of carbon dioxide and moisture is preferably referred to as carbonation.
  • the decorated, mineral composite body produced using the method according to the invention has a barrier against acidic substances and protection against driving and loosening attacks.
  • a driving attack occurs when the substances affecting the concrete form new reaction products with a significantly larger volume when they react with the cement paste, and in some cases also with the aggregates. The greater space requirement can then lead to the concrete being blasted out from the inside.
  • a typical example of this is sulfate blowing.
  • sulphate-containing gases or solutions act on concrete, the reaction between sulphates and the tricalcium aluminate of the cement paste (C3A) can primarily lead to the formation of ettringite.
  • the volume of the reaction products can increase to eight times the original volume of the starting materials and the concrete is blasted out from the inside. This damage often occurs in sewers concrete on.
  • bacterial decomposition of the sulphur-containing organic substances (such as proteins) contained in the sewage produces hydrogen sulfide gas, which smells like rotten eggs. This gas can be oxidized to sulfates by other bacteria or by the oxygen in the air, and these can cause sulfate drift.
  • the decorated, mineral composite body preferably produced with the method according to the invention also preferably has a barrier against frost-defrosting agents, for example de-icing salts containing chloride ions.
  • At least one first multilayer film and at least one second multilayer film can be used in the method according to the invention, the at least first multilayer film being provided with the side of the carrier layer of the at least first multilayer film facing away from the at least one polymer-containing primer layer on the at least one inner surface of the provided Form element, preferably formwork, is arranged, wherein in step b) the at least one polymer-containing primer layer of the at least first multi-layer film is at least partially brought into contact with the flowable or plastically deformable mineral building material mixture, and wherein the at least second multi-layer film in and/or after step c) with a side facing away from the carrier layer of the at least one polymer-containing primer layer of the at least second multi-layer film is arranged on the dimensionally stable, mineral green body, with a decorated, dimensionally stable, mineral green body being obtained through the at least partial solidification of the mineral building material mixture.
  • the at least one multilayer film is more preferably arranged with the side of the at least one polymer-containing primer layer facing away from the carrier layer on the dimensionally stable, mineral green body before step d).
  • the method according to the invention gives, preferably in or after step d), a decorated mineral composite body which contains an at least partially hardened mineral substrate and at least one transfer layer which is at least partially arranged on at least one surface of the mineral substrate and contains at least one decorative element. includes or consists of, wherein the mineral substrate facing side of the transfer layer by at least one polymer-containing organic Primer layer is formed, which is at least positively connected to the mineral substrate.
  • the mineral substrate of the decorated, mineral composite body preferably comprises or consists of at least one solidified, preferably hardened, mineral building material, optionally at least one aggregate and/or at least one non-volatile additive and optionally at least one reinforcement element.
  • a mineral building material is preferably an inorganic, non-metallic material made up of at least partially crystalline components.
  • These can be natural minerals, such as natural stone, sand, clay or loam, or a shaped mixture of materials made from sieved and/or ground minerals, which are given the desired strength, preferably in the presence of water, by crystallization of at least one mineral binder.
  • step b) of the method according to the invention a flowable or plastically deformable mineral building material mixture comprising water and at least one mineral binder is used, which at least partially solidifies in step c) of the method according to the invention to obtain a dimensionally stable, mineral green body.
  • the at least partial solidification of the mineral building material mixture can also be referred to as setting, wherein the solidification, particularly in the case of cement paste, represents the defined increase in viscosity due to water binding, preferably the incorporation of water of crystallization, in concrete or mortar.
  • the at least partial solidification of the mineral building material mixture preferably gives a mineral green body which is at least dimensionally stable.
  • the green body preferably has a lower strength than the at least partially cured mineral composite body.
  • the strength of mineral building materials is caused by the, preferably exothermic, reaction of crystallization of components of the used mineral binder, such as clinker components of cement, preferably with water absorption. During this process, crystal needles grow, which can interlock tightly.
  • the at least one mineral binder used in the method according to the invention is preferably selected from the group consisting of calcium silicate hydrates, cement, lime, clay, gypsum, loam, magnesia binder and combinations thereof
  • the at least one mineral binder preferably comprises or consists of a hydraulic binder, a non-hydraulic binder or a mixture thereof.
  • a non-hydraulic binder is preferably an inorganic, non-metallic, finely ground material which upon contact, preferably mixing, with water sets in air.
  • Non-hydraulic binders are not water resistant when hardened.
  • a non-hydraulic binder is preferably quicklime, which hardens in the presence of water with the simultaneous supply of air, since the carbon dioxide from the air forms carbonic acid with water, which is used to carbonate the calcium hydroxide (slaked lime).
  • magnesia binder is preferably magnesia binder, which can be prepared by mixing caustic burnt magnesite (magnesia, MgO) with magnesium chloride (MgCl 2 ) dissolved in water. Hardening occurs through the mutually penetrating and matting fine crystal needles of the magnesium hydroxide that is formed. The hardening is completed in a few hours.
  • a hydraulic binder is preferably an inorganic, non-metallic, finely ground substance which, after it has been brought into contact, preferably mixed, with water, as a result of chemical reactions with the water, independently solidifies and hardens and, after hardening, preferably remains solid and dimensionally stable even under water.
  • Hydraulic binders consist of compounds between a non-hydraulic base, e.g. lime (CaO), magnesia (MgO) or mixtures thereof, and so-called hydraulic factors, e.g. silicon dioxide (SiO 2 ), aluminum oxide/alumina (Al 2 O 3 ), iron oxide (Fe 2 O 3 ) or mixtures thereof.
  • a non-hydraulic base e.g. lime (CaO), magnesia (MgO) or mixtures thereof
  • hydraulic factors e.g. silicon dioxide (SiO 2 ), aluminum oxide/alumina (Al 2 O 3 ), iron oxide (Fe 2 O 3 ) or mixtures thereof.
  • the hydraulic binders include, for example, all types of cement according to DIN EN 197-1:2011-11 ("Cement - Part 1: Composition, requirements and conformity criteria of normal cement”; German version EN 197-1:2011, issue date 2011-11), DIN 1164-10:2013-03 ("Cement with special properties - Part 10: Composition, requirements and proof of conformity of cement with a low effective alkali content", issue date 2013-03) and DIN 1164-11:2003-11 (“Cement with special properties - Part 11: Composition, requirements and proof of conformity of cement with reduced setting", issue date 2003-11) as well as hydraulic lime according to DIN EN 459-1:2015-07 ("Building lime - Part 1: Terms, requirements and conformity criteria" German version EN 459-1:2015, issue date 2015-07).
  • the at least one mineral binder is selected from the group consisting of Portland cement, Portland slag cement, Portland silica fume cement, Portland pozzolan cement, Portland fly ash cement, Portland shale cement, Portland limestone cement, Portland composite cement, blast furnace cement, pozzolan cement, composite cement, alumina cement and mixtures thereof.
  • a hydraulic binder comprises calcium oxide (CaO) and silica (SiO 2 ) in a CaO/SiO 2 molar ratio greater than 1.5.
  • a latent hydraulic substance has calcium oxide (CaO) and silicon dioxide (SiO 2 ) in a CaO/SiO 2 molar ratio ranging from 0.5 to 1.5.
  • Latent-hydraulic substances harden hydraulically after they have been finely ground and brought into contact, preferably mixing, with water, since their reaction with water without other additives through hydration produces strength-forming, calcareous hydration products.
  • latently hydraulic substances are not independent binders, they are counted among the concrete additives when used as a starting material for concrete.
  • Pozzolans are siliceous or siliceous and alumina-containing materials.
  • pozzolan In contrast to latently hydraulic substances, pozzolan contains only little calcium oxide (CaO). Pozzolans have calcium oxide (CaO) and silicon dioxide (SiO 2 ) in a CaO/SiO 2 molar ratio of less than 0.5.
  • Pozzolan can therefore only form hardenable hydration products in conjunction with a substance that releases calcium hydroxide (Ca(OH) 2 ) after it has been brought into contact, preferably mixed, with water.
  • Natural pozzolana are rocks and soils that are preferably dried at temperatures of no more than about 150 °C. Like trass, lava, pozzolan and santorini, they are mostly of volcanic origin.
  • Rocks and soils are referred to as artificial or natural tempered pozzolan that are technically calcined (tempered) at a higher temperature in order to develop sufficient pozzolanic reactivity.
  • Tempered clay, brick dust, silica fume and fly ash can exhibit pozzolanic properties.
  • Important pozzolans are fly ash, brick dust, silica fume, rice hull ash, phonolite, calcined clay, and metakaolin.
  • pozzolana also belong to the concrete additives.
  • the mineral building material mixture preferably includes or consists of concrete, mortar, sand-lime brick, ceramics or a combination thereof.
  • ceramic is preferably understood to mean silicate ceramic, oxide ceramic, non-oxide ceramic and combinations thereof, preferably silicate ceramic and oxide ceramic.
  • the mineral building material mixture comprises concrete or mortar, the at least one mineral binder comprising or consisting of cement, and the mineral building material mixture also comprising aggregate.
  • aggregate is preferably understood to mean a mixture of broken or unbroken grains of the same or different sizes made from natural and/or artificial mineral substances.
  • the at least one multi-layer film is preferably arranged before step b) with the side of the carrier layer facing away from the at least one polymer-containing primer layer on at least one inner surface of the formwork, so that the at least one polymer-containing primer layer of the multi-layer film preferably points away from the at least one inner surface of the formwork.
  • step b) the at least one polymer-containing primer layer of the carrier layer is at least partially brought into contact with the free-flowing, mineral building material mixture, with a decorated, dimensionally stable, mineral green body being obtained in step c) through the at least partial solidification of the mineral building material mixture , in which the at least one polymer-containing primer layer of the multi-layer film is preferably positively connected to the at least partially solidified mineral building material mixture.
  • a decorated, mineral composite body is obtained by at least partial hardening of the mineral building material mixture.
  • Concrete is preferably a building material that is mixed as a dispersion with the addition of liquid, preferably water, from a binder and aggregates.
  • the hardened concrete is also referred to as artificial stone in some contexts.
  • Concrete preferably contains cement as a binder and aggregate as an aggregate.
  • the added water preferably initiates the chemical setting process.
  • concrete additives and/or concrete additives can be added to the building material mixture.
  • the water is preferably chemically bound for the most part.
  • topping concrete in-situ concrete, pumped concrete, spun concrete, shotcrete, stamped concrete, rolled concrete, underwater concrete, vacuum concrete, screed concrete, blue concrete, fiber and textile concrete
  • glass-foam concrete glass-reinforced concrete, high-strength and ultra-high-strength concrete (UHFB), infra-light concrete and ultra-light concrete
  • concrete concrete air-entrained concrete (LP-concrete)/foam concrete, lean concrete, eco-concrete, paper concrete, polymer concrete and mineral cast, recycled concrete, acid-resistant concrete, self-cleaning concrete, self-compacting concrete (SVB), exposed, structural, textured and photo concrete, chippings and drainage concrete
  • Reinforced concrete prestressed concrete, steel fiber concrete, translucent concrete (Translucent concrete), aggregate concrete, water-impermeable concrete (WU concrete), fresh concrete, colored concrete, structurally dense concrete, no-fines lightweight concrete, heavy concrete/radiation protection concrete, wood concrete, carbon concrete
  • Mortar is preferably a building material that consists of a binder, for example lime or cement, aggregate with preferably a maximum grain size of 4 mm and added water, possibly also of concrete additives and additives, and which hardens as a result of the chemical reaction of the binder.
  • a binder for example lime or cement
  • aggregate with preferably a maximum grain size of 4 mm and added water, possibly also of concrete additives and additives, and which hardens as a result of the chemical reaction of the binder.
  • Suitable mortars are, for example, masonry mortar, plaster mortar, fire protection mortar, synthetic resin mortar, screed mortar, grouting mortar, swelling mortar, water mortar and mineral sealing slurries or combinations thereof.
  • preformed building materials such as stone or brick
  • non-preformed building materials such as concrete or mortar
  • aerated concrete is a steam-hardened building material, preferably with a bulk density of 300 kg/m 3 to 800 kg/m 3 , which can preferably be produced from the raw materials burnt lime (CaO) as a mineral binder, water and quartz sand, with a small amount of a pore-forming agent, preferably aluminum powder or paste.
  • the building material mixture is preferably poured into a mold element in which the metallic, finely divided aluminum develops hydrogen gas in the alkaline suspension.
  • quicklime (CaO) and sand are preferably mixed with the addition of water.
  • the quicklime is preferably converted to calcium silicate hydrate with water
  • the mixture can be formed into a dimensionally stable green body, preferably by pressing.
  • the mineral building material mixture comprises a ceramic, preferably silicate ceramic, preferably porcelain, oxide ceramic and non-oxide ceramic, preferably silicate ceramic and oxide ceramic, or consists of it, with the at least one mineral binder Clay mineral, preferably kaolinite, comprises or consists of.
  • a dimensionally stable, mineral green body is preferably obtained in step c) by pressing, slip casting, injection molding, film casting, modeling and/or extrusion, the at least one multilayer film in and/or after step c) having the at least one polymer-containing primer layer on at least one surface of the dimensionally stable, mineral green body at least is partially arranged to obtain a decorated, dimensionally stable, mineral green body.
  • the decorated, dimensionally stable, mineral green body is preferably fired, preferably at a temperature of 850° C. or more for a period of at least 12 hours, to give a decorated, mineral composite body.
  • the at least one multilayer film comprises at least one fireproof decorative element, preferably one or more fireproof pigments and/or one or more molded surface reliefs.
  • a multilayer film to be used according to the invention has a carrier layer and a transfer layer which is arranged on the carrier layer and contains at least one of the aforementioned decorative elements, the transfer layer having at least one polymer-containing primer layer on the side facing away from the carrier layer.
  • the inventors have found that at least partial solidification of the mineral building material mixture forms a dimensionally stable, mineral green body which has pores into which the at least one polymer contained in the polymer-containing primer layer, comprising at least one dissociable, Functional group, preferably after dissociation at least one functional group capable of dissociation, can "interlock" mechanically.
  • the bond strength preferably correlates with the curing time, since the bond strength is lower after one or two days than after several days.
  • the adhesive strength of the multi-layer film and/or the transfer layer of the multi-layer film on the solidified building material mixture or the composite body according to the invention can be checked with a cross-cut according to DIN EN ISO 2409: 2013-06 (coating materials - cross-cut test (ISO 2409: 2013), German version of EN ISO 2409:2013, issue date: 2013-06).
  • a polymer molecule contained in the at least one polymer-containing primer layer which has at least one functional group capable of dissociation, after dissociation of at least one functional group capable of dissociation, preferably with the formation of at least one anionic functional group, more preferably anionic acid Group, adheres particularly well to the flowable or plastically deformable mineral building material mixture or to the dimensionally stable mineral green body obtained by at least partially solidifying the mineral building material mixture.
  • the at least one polymer having at least one functional group capable of dissociation after dissociation of at least one of the functional groups capable of dissociation at the molecular level preferably has at least one anionic functional group, for example a deprotonated acid group, the at least an anionic, functional group of the polymer with metal ions, in particular Ca 2+ ions, of the mineral building material mixture, preferably in the presence of bound water, can enter into coordinate bonds.
  • the aqueous polymer dispersion or polymer solution used to produce the polymer-containing primer layer has a pH of 1.0 to 9.0, preferably 1.5 to 7.0, preferably 2.0 to 6.0, preferably from 2.5 to 5.5, preferably from 3.0 to 5.0, measured in each case at a temperature of 25° C. and a pressure of 1013 mbar.
  • a non-aqueous polymer dispersion or polymer solution can be used to produce the polymer-containing primer layer, which, in addition to the at least one polymer having at least one functional group capable of dissociation, preferably also contains at least one organic solvent, which, for example, consists of alcohols, carboxylic acid esters, ethers, ketones , alkanes, aromatic hydrocarbons, halogenated aliphatic hydrocarbons, lactones, lactams, nitriles, nitro compounds, tertiary carboxamides, sulfoxides, glycol ethers or mixtures thereof.
  • at least one organic solvent which, for example, consists of alcohols, carboxylic acid esters, ethers, ketones , alkanes, aromatic hydrocarbons, halogenated aliphatic hydrocarbons, lactones, lactams, nitriles, nitro compounds, tertiary carboxamides, sulfoxides, glycol ethers or mixtures thereof
  • the at least one polymer having at least one functional group capable of dissociation, of the at least one polymer-containing primer layer, independently of one another, comprises at least one free amino group and/or at least one free hydroxy group and/or at least one free acid group, which preferably is selected from the group consisting of carboxy group, sulfonic acid group, which can also be referred to as sulfo group, sulfuric acid monoester group, phosphonic acid group, phosphoric acid monoester group and combinations thereof, preferably carboxy group, sulfonic acid group, phosphonic acid group and combinations thereof, more preferably carboxy group, sulfonic acid group and combinations thereof preferably carboxy group, and/or at least one blocked acid group, which is preferably selected from the group consisting of carboxylic acid ester group, carboxylic acid anhydride group, carboxylic acid halide group, sulfonic acid ester group, sulfonic acid anhydride group, sulfonic acid halide group
  • the at least one polymer having at least one dissociative functional group of the at least one polymer-containing primer layer independently comprises at least one free acid group, which is preferably selected independently from the group consisting of carboxy group, sulfonic acid group , which can also be referred to as sulfo group, sulfuric acid monoester group, phosphonic acid group, phosphoric acid monoester group and combinations thereof, preferably carboxy group, sulfonic acid group, phosphonic acid group and combinations thereof, more preferably carboxy group, sulfonic acid group and combinations thereof, more preferably carboxy group, and/or at least one capped acid group, which is preferably each independently selected from the group consisting of carboxylic acid ester group, carboxylic acid anhydride group, carboxylic acid halide Group, sulfonic acid ester group, sulfonic acid anhydride group, sulfonic acid halide group, phosphonic acid ester group and combinations thereof, more preferably carboxylic acid ester
  • a polymer having at least one free, anionic, functional group can, for example, from the group consisting of anionically functionalized epoxy polymers and copolymers, anionically functionalized acrylic polymers and - Copolymers, anionically functionalized methacrylic polymers and copolymers, anionically functionalized polyurethane polymers and copolymers and mixtures thereof, preferably anionically functionalized acrylic polymers, anionically functionalized methacrylic polymers, anionically functionalized polyurethane polymers, copolymers thereof and mixtures thereof, to be chosen.
  • Anionically functionalized polymers and copolymers can be incorporated into the at least one polymer, for example via suitable chain extenders which have appropriate ionic groups, in order to stabilize this as a particle dispersed in water.
  • a typical representative of polyurethane polymers is, for example, dimethylolpropionic acid for carboxy functionality and diolsulfonates for pendant sulfonic acid groups.
  • the polymer obtained is preferably permanently hydrophilic and more preferably is easily dispersed.
  • anionically functionalized epoxy resins can be derived from one or more epoxy resins.
  • Anionic functionalized groups can be introduced into epoxy resin molecules by different methods. Typically, epoxy resins contain hydroxy groups as well as epoxy groups. These groups can be reacted with various reagents containing the desired anionic functional group or precursor thereof, for example by varying the ratio of dicarboxylic acid to starting epoxy resin.
  • Another means of adding anionic functional groups to the epoxy resin is by reacting the epoxy resin with a functionalizing agent containing at least one anionic functional group or a precursor thereof and at least one functional group capable of reacting with epoxy groups and/or To react to hydroxyl groups, the epoxy resin to be reacted preferably containing hydroxyl groups.
  • Non-exclusive examples of such functionalizing agents include compounds having at least one sulfonate functionality and/or at least one carboxylate functionality, and more preferably at least one aromatic hydroxyl functionality.
  • alkaline metal salts of hydroxybenzenesulfonic acid and hydroxybenzoic acid are representative compounds of this type.
  • the starting epoxy resin can be derived by reaction with phosphorylating, sulphating and/or sulphonating reagents such as superphosphoric acid, sulfuric acid and the like
  • Polyacrylates and polymethacrylates preferably have free deprotonated carboxylate groups.
  • Suitable polymer dispersions are, for example, under the type designation NeoCryl® , which are aqueous polyacrylate polymer and copolymer dispersions, and NeoRez® , which are aqueous polyurethane polymer and copolymer dispersions, commercially available from DSM Coating Resins BV (Zwolle, NL).
  • free acid group is preferably understood as meaning a covalently bonded functional group which can preferably donate at least one proton.
  • a free acid group is uncharged and more preferably is each independently selected from the group consisting of carboxy group, sulfonic acid group, sulfuric acid monoester group, phosphonic acid group, phosphoric acid monoester group, and combinations thereof, preferably carboxy - group, sulfonic acid group, phosphonic acid group and combinations thereof, more preferably carboxy group, sulfonic acid group and combinations thereof, more preferably carboxy group, is selected.
  • the at least one polymer having at least one free acid group is more preferably selected from the group consisting of epoxy polymers and copolymers each having at least one free acid group, acrylic polymers and - Copolymers each having at least one free acid group, methacrylic polymers and copolymers each having at least one free acid group, polyurethane polymers and copolymers each having at least one free acid group and mixtures thereof, preferably acrylic polymers each having at least a free acid group, methacrylic polymers each having at least one free acid group, polyurethane polymers each having at least one free acid group, copolymers thereof and mixtures thereof.
  • Suitable polymers with at least one free acid group can be prepared, for example, from the aforementioned polymers with at least one free anionic functional group, preferably by changing the pH, for example by acidification.
  • Suitable polymers and polymer dispersions with at least one free acid group are available commercially, for example, from MÜNZING CHEMIE GmbH (Abstatt, DE) under the type designation WÜKOSEAL® , preferably WÜKOSEAL® VP Ku, which is a vinyl acetate-ethylene copolymer for example under the brand name Carbopol® , which are polyacrylic acids commercially available from Lubrizol Corporation (Wickliffe, Ohio, US).
  • the at least one polymer having at least one capped acid group is more preferably selected from the group consisting of epoxy polymers and copolymers each having at least one capped acid group, acrylic polymers and copolymers each having at least one capped acid group, methacrylic polymers and copolymers each having at least one capped acid group, polyurethane polymers and copolymers each having at least one capped acid group and mixtures thereof, styrenic polymers and copolymers each having at least one capped acid group , preferably acrylic polymers and copolymers each having at least one blocked acid group, methacrylic polymers and copolymers each having at least one blocked acid group, polyurethane polymers and copolymers each having at least one blocked acid group, styrene polymers and copolymers each having at least one capped acid group, and mixtures thereof.
  • the term “disguised acid group” is preferably understood to mean a functional group which more preferably has at least one acid group, preferably in the form of the deprotonated anion of the corresponding acid group.
  • Suitable polymers with at least one capped acid group which is preferably selected independently from the group consisting of carboxylic acid ester group, carboxylic acid anhydride group, carboxylic acid halide group, sulfonic acid ester group, sulfonic anhydride group, sulfonic acid halide group, phosphonic acid ester group and combinations thereof, more preferably carboxylic acid ester group, carboxylic acid anhydride group, sulfonic acid ester group and combinations thereof, more preferably carboxylic acid ester group, carboxylic acid anhydride group and combinations thereof, more preferably carboxylic acid ester group, sulfonic acid ester group and combinations thereof, more preferably carboxylic acid ester group are known to those skilled in the art and can be prepared, for example, by synthetic methods known in the art.
  • polymers with at least one ester group preferably carboxylic acid ester group, sulfonic acid ester group, phosphonic acid ester group, combinations thereof or mixtures thereof
  • polymers with at least one ester group can be prepared by reacting a polymer with at least one corresponding acid group, preferably carboxy group, sulfonic acid group, phosphonic acid group, combinations thereof or mixtures thereof, and/or at least one corresponding acid halide group, preferably carboxylic acid chloride group, sulfonic acid chloride group, or combinations thereof, and/or at least one corresponding acid anhydride group, preferably carboxylic acid anhydride, sulfonic acid anhydride or combinations thereof
  • at least one alcohol preferably aliphatic Alcohol having 1 to 6 carbon atoms, aromatic alcohol having 6 or more carbon atoms or mixtures thereof, more preferably aliphatic alcohol having 1 to 3 carbon atoms, can be prepared by methods known to those skilled in the art, for example using an acid as a catalyst.
  • Polymers having at least one acid halide group preferably a carboxylic acid halide group, which can also be referred to as a halocarbonyl group, a sulfonic acid halide group, which can also be referred to as a halosulfonyl group, or combinations thereof, are known to those skilled in the art.
  • suitable acid halide groups from the group consisting of the carboxylic acid chloride group, which can also be referred to as a chlorocarbonyl group, a sulfonic acid chloride group, which can also be referred to as a chlorosulfonyl group, and combinations, and can also be selected according to im Synthesis methods known in the prior art can be prepared.
  • the at least one functional layer 14 arranged between the at least one polymer-containing primer layer 15 and the carrier layer 10, 10' can preferably also contain at least one additive, which is preferably selected from the group consisting of hydrophobing agents, leveling additives, defoamers, colorants, preferably selected from dyes, organic pigments, inorganic pigments and mixtures thereof, fillers, rheology additives, plasticizers, stabilizers, light stabilizers, antioxidants, flame retardants, reinforcing materials and mixtures thereof.
  • at least one additive is preferably selected from the group consisting of hydrophobing agents, leveling additives, defoamers, colorants, preferably selected from dyes, organic pigments, inorganic pigments and mixtures thereof, fillers, rheology additives, plasticizers, stabilizers, light stabilizers, antioxidants, flame retardants, reinforcing materials and mixtures thereof.
  • the at least one shaped element 30 used in the method according to the invention comprises at least one outer surface and at least one inner surface 30, wherein the at least one inner surface 31 of the shaped element 30 can preferably have a two-dimensional or three-dimensional geometric shape. Alternatively or additionally, the inner surface 31 of the shaped element 30 can also have a structuring in the form of a macroscopic and/or microscopic structure.
  • the at least one multilayer film 1, 1' to be used according to the invention can preferably be at least partially decorated by at least one decorative roller or contain at least one decorative pattern.
  • a protective layer 18 optionally arranged on the side of the at least one polymer-containing primer layer 15 facing away from the carrier layer 10, 10' is preferably applied in the method according to the invention in alternative I) before the at least one polymer-containing one is brought into contact at least partially Primer layer 15 with the free-flowing or plastically deformable mineral building material mixture, and/or in alternative II) preferably before arranging the at least one polymer-containing primer layer 15 on the dimensionally stable, mineral green body 3a, at least partially, preferably completely, removed.
  • a decorated, dimensionally stable, mineral green body 3 preferably comprises an at least partially solidified mineral building material mixture and at least one transfer layer 13, 13', which is at least partially arranged on at least one surface of the green body 3 and contains at least one decorative element, the one facing the green body 3 Side of the transfer layer 13, 13 'is formed by at least one polymer-containing primer layer 15 which is at least positively connected to the green body 3.
  • at least one carrier layer 10, 10' is also arranged on the at least one transfer layer 13, 13' on the side of the transfer layer 13, 13' facing away from the green body 3.
  • a decorated mineral composite body 2 according to the invention in particular produced according to a method of claims 1 to 26, comprises a mineral substrate S and at least one transfer layer 13, 13', which is at least partially arranged on at least one surface of the substrate S and contains at least one decorative element.
  • the side of the transfer layer 13, 13" facing the substrate S being formed by at least one polymer-containing primer layer 15 which is connected to the substrate S at least in a form-fitting manner.
  • the mineral substrate S of the mineral composite body 2 decorated according to the invention preferably comprises at least one at least partially hardened mineral building material selected from the group consisting of concrete, mortar, sand-lime brick, ceramic and combinations thereof, or consists of it.
  • At least one carrier layer 10, 10' is arranged on the at least one transfer layer 13, 13', the at least one transfer layer 13, 13" and the at least one carrier layer 10, 10' form a multilayer film 1, 1', which is preferably designed as a laminating film.
  • a multilayer film 1, 1' which is preferably designed as a laminating film, can preferably be smaller than the at least one surface of the substrate S on which the transfer layer 13, 13', which contains at least one decorative element, is at least partially arranged, preferably bonded, be designed.
  • the layers produced using these methods are, for example, reflection layers, conductive layers, barrier layers, decorative layers, which can each be present over the entire surface and/or partially.
  • At least one decorative layer is vapor-deposited onto the replication layer, preferably in areas or over the entire surface, after molding an optically active surface structure in a replication layer.
  • At least one decorative layer over the entire surface, followed by a region-wise removal by means of known methods such as washing methods or lift-off lacquers or etching methods or mask exposure methods with the aid of a photoresist layer.
  • the at least one polymer-containing primer layer 15 of the transfer layer 13, 13' is first applied to the transfer layer 10, 10', which can comprise at least one carrier layer made of a polyester, a polyolefin, or a combination thereof, in particular made of PET, by at least one of the the aforementioned printing and/or casting processes are arranged or applied, with the at least one polymer-containing primer layer 15 being more preferably applied with an application weight in a range from 0.5 g/m 2 to 500 g/m 2 , preferably from 1 g/m 2 to 50 g/m 2 , preferably from 5 g/m 2 to 25 g/m 2 , preferably from 9 g/m 2 to 15 g/m 2 , in each case based on the total weight of all components of the polymer-containing primer layer 15.
  • the at least one polymer-containing primer layer 15 is produced using an aqueous polymer dispersion which has a pH of 1.0 to 9.0, preferably 1.5 to 7.0, preferably 2.0 to 6. 0, preferably from 3.0 to 5.0, measured in each case at a temperature of 25° C. and a pressure of 1013 mbar.
  • a PET carrier coated with a layer of at least 50 nm thick of a montan ester wax (thickness of the PET carrier from 5 ⁇ m to 150 ⁇ m, preferably from 7 ⁇ m to 100 ⁇ m) as a carrier layer was coated with an aqueous primer made of WÜKOSEAL ® VP Ku (MÜNZING CHEMIE GmbH), which is an aqueous dispersion of a vinyl acetate-ethylene copolymer with a pH value according to the manufacturer's specification of 4.5 ⁇ 1, in a mixture of water and isopropanol, solids approx. 15%, typically with an application weight of 10 g/m 2 .
  • WÜKOSEAL ® VP Ku MÜNZING CHEMIE GmbH
  • the PET carrier was then detached from the concrete, leaving the transfer liner adhered to the concrete and forming a smooth coating on the composite.
  • a knife and preferably a template were used to make 6 vertical cuts and 6 horizontal cuts (at an angle of 90° to the vertical cuts) in the coating down to the substrate.
  • the width of the cut depended on the layer thickness of the coating. In the case of coatings with a layer thickness of less than 60 ⁇ m, the distance between the cuts is preferably about 1 mm.
  • a transparent adhesive tape or a crepe adhesive tape with an adhesive strength of 6 N/25 mm to 10 N/25 mm was stuck onto the resulting square of the cuts (measuring area). This was peeled off at an angle of 60° in a time of 0.5 to 1 second.
  • the tests showed that the multilayer film and/or the transfer layer of the multilayer film remained largely completely on the solidified building material mixture and only the adhesive strip was pulled off again.
  • the force measured was between 400 cN and 1000 cN.
  • the adhesive force between the multilayer film and/or the transfer layer of the multilayer film to the solidified building material mixture should therefore be higher than this measured adhesive force, since after detachment of the adhesive strip from the multilayer film and/or the transfer layer under this measured adhesive force there are still no defects in the multilayer film and/or the transfer layer of the multilayer film.
  • the rupture edges of the specimens were examined in the REM images.
  • the SEM images were each recorded with the following parameters: 8 kV voltage, 20 mm sample distance, spot size 39, viewing angle 80°.

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EP21713902.1A 2020-04-08 2021-03-17 Verfahren zur herstellung eines dekorierten, mineralischen verbundkörpers, dekorierter, mineralischer verbundkörper und verwendung einer mehrschichtfolie Active EP4132894B1 (de)

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JP2967515B2 (ja) * 1996-08-28 1999-10-25 大日本印刷株式会社 耐久性グラビアインキ並びにそれを用いた化粧材及び転写シート
JP3827843B2 (ja) 1997-12-03 2006-09-27 大日本印刷株式会社 熱転写受像シート
WO2002036524A1 (en) * 2000-11-01 2002-05-10 Valspar Sourcing, Inc. Abrasion resistant coating for stacks of fiber cement siding
ATE307788T1 (de) * 2001-12-22 2005-11-15 Henkel Kgaa Verfahren zur beschichtung eines zementhaltigen formteiles
AU2007209879B2 (en) * 2006-01-31 2012-04-26 Valspar Holdings I, Inc Coating system for cement composite articles
EP1829699A1 (de) * 2006-03-03 2007-09-05 Helmut Szynka Verfahren zum Aufbringen eines Farbdekors auf ein Substrat
EP2190938A1 (de) * 2007-09-12 2010-06-02 Basf Se Verfahren zur herstellung von verbunden aus mineralischen körpern und kunststoffen
EP2299005A1 (de) 2009-09-21 2011-03-23 Sika Technology AG Wasserdichte Membran
FR3001727B1 (fr) * 2013-02-06 2015-01-23 Lafarge Sa Liant hydraulique
CN104343219A (zh) * 2013-07-30 2015-02-11 吕孟龙 无机聚合物复合板
DE102015115748A1 (de) * 2015-09-17 2017-03-23 Kennwert RD GmbH Verfahren zur Herstellung von integrierten Schaltungen auf bzw. in Beton
DE102015223197A1 (de) * 2015-11-24 2017-05-24 Dresdner Lackfabrik Novatic Gmbh & Co. Kg Beschichtungssystem für Betonoberflächen
CN108290378B (zh) * 2015-12-23 2021-10-29 Sika技术股份公司 具有矿物粘结剂组分的接触层
EP3239109A1 (en) * 2016-04-28 2017-11-01 Omya International AG Surface-treated mineral material and its use in water purification
PL3315316T3 (pl) 2016-10-27 2021-06-14 Akzenta Paneele + Profile Gmbh Sposób wytwarzania dekorowanego panelu ściennego lub podłogowego
DE102017104658B4 (de) * 2017-03-06 2022-06-23 Leonhard Kurz Stiftung & Co. Kg Verfahren zur Herstellung eines Decals und ein Decal sowie ein Verfahren zum Dekorieren von Oberflächen von Gegenständen
DE102018125312A1 (de) 2018-10-12 2020-04-16 Leonhard Kurz Stiftung & Co. Kg Verfahren zur Herstellung eines dekorierten, mineralischen Verbundkörpers, dekorierter, mineralischer Verbundkörper und Verwendung einer Mehrschichtfolie

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DE102020109909A1 (de) 2021-10-14
PL4132894T3 (pl) 2023-11-27
TWI896623B (zh) 2025-09-11
US20230150892A1 (en) 2023-05-18
US12600684B2 (en) 2026-04-14
TW202204291A (zh) 2022-02-01
WO2021204503A1 (de) 2021-10-14
ES2956554T3 (es) 2023-12-22
CN115397789B (zh) 2023-12-08
CN115397789A (zh) 2022-11-25

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